Key responsibilities as Study Coordinator:
- CRA Support: Schedule appointments for CRA at the site; assist CRA with questions regarding study procedures, documentation, and associated protocols.
- Document Administration: Collect signatures for study documentation; oversee training and responsibility logs; maintain and update clinical trial trackers; track and review amendments, assigning those requiring changes to the appropriate team member.
- Study Medication Management: Oversee receipt, return, and transfer of study medication; ensure proper accountability and storage with the help of site pharmacist; manage drug return counts; report temperature excursions to the sponsor and monitor quarantine procedures.
- **Invoicing/Budgets: Identify and manage patient study reimbursement from the sponsor and raise invoices; handle invoicing for clinical trial-related costs.
- Systems Management: Ensure internal systems are up to date and deadlines are met by the team; follow up on any issues related to system forms and study specifications.
- General Responsibilities: Regularly liaise with senior clinical staff to update and progress clinical trial work; support audit and inspection activities.
Job Types: Part-time, Casual, Freelance, Contract
Pay: $55.00 – $60.00 per hour
Work Location: In person
